Comparison of Intrathecal Injection of same dose of Fentanyl at Different Rates in Patients undergoing Elective LSCS
Phase 4
- Conditions
- Health Condition 1: O- Medical and Surgical
- Registration Number
- CTRI/2022/04/042039
- Lead Sponsor
- Sawai Man Singh Medical College and Hospitals
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
Patients undergoing Elective LSCS under spinal anaesthesia
Exclusion Criteria
1)ASA Grade 3&4,2)Parturients with complicated pregnancies such as those with pre-eclampsia,pregnancy induced hypertension,gestational diabetes,abnormal placenta(placenta previa),multiple gestation,BMI >35 or <22, major systemic diseases(cardiac, renal, liver)
3)Parturients with a need for emergency CS.
4)Parturientswho are allergic to drugs used in this study
5)Parturients contraindicated for spinal anaesthesia
6)Parturients who refused spinal anaesthesia.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Total duration of post operative analgesiaTimepoint: until 6hrs postoperatively
- Secondary Outcome Measures
Name Time Method Dose of rescue analgesia usedTimepoint: postoperatively every 30 min until 6hrs;duration of motor blockTimepoint: time taken to return to a bromage score of 0;Haemodynamic Parameters (systolic BP,Diastolic BP, Mean arterial pressure, Heart Rate,spo2)Timepoint: baseline,2min,4min,6min,8min ,10 min,15min, 20 min and then every 10 min till 60 min;Intensity of Post operative Pain assesesd by VAS ScoreTimepoint: postoperatively every 30 min until 6 hrs;Intra operative HypotensionTimepoint: intraoperatively;onset of motor blockTimepoint: time taken to achieve a Bromage score of 3;onset of sensory block and highest level of sensory blockTimepoint: after 10 min;Spinal anaesthesia related complicationsTimepoint: intraoperatively